Primidone - 0615-7738-39 - (Primidone)

Alphabetical Index


Drug Information of Primidone

Product NDC: 0615-7738
Proprietary Name: Primidone
Non Proprietary Name: Primidone
Active Ingredient(s): 250    mg/1 & nbsp;   Primidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Primidone

Product NDC: 0615-7738
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084903
Marketing Category: ANDA
Start Marketing Date: 19781201

Package Information of Primidone

Package NDC: 0615-7738-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7738-39)

NDC Information of Primidone

NDC Code 0615-7738-39
Proprietary Name Primidone
Package Description 30 TABLET in 1 BLISTER PACK (0615-7738-39)
Product NDC 0615-7738
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19781201
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PRIMIDONE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Primidone


General Information